MEI, DAVIDE
MEI, DAVIDE
Neuroscienze, Psicologia, Area del Farmaco e Salute del Bambino (NEUROFARBA)
A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations
2017 Zhu X, Padmanabhan R, Copeland B, Bridgers J, Ren Z, Kamalakaran S, O'Driscoll-Collins A, Berkovic SF, Scheffer IE, Poduri A, Mei D, Guerrini R, Lowenstein DH, Allen AS, Heinzen EL, Goldstein DB
Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course
2019 Alessandro Esposito, Antonio Falace, Matias Wagner, Moran Gal, Davide Mei, Valerio Conti, Tiziana Pisano, Davide Aprile, Maria Sabina Cerullo, Antonio De Fusco, Silvia Giovedì, Annette Seibt, Daniella Magen, Tilman Polster, Ayelet Eran, Sarah L Stenton, Chiara Fiorillo, Sarit Ravid, Ertan Mayatepek, Hava Hafner, Saskia Wortmann, Erez Y Levanon, Carla Marini, Hanna Mandel, Fabio Benfenati, Felix Distelmaier, Anna Fassio, Renzo Guerrini
Bilateral Perisylvian Polymicrogyria, Intellectual Disability and Nephronophthisis Associated With Compound Heterozygous Pathogenic Variants in the CEP83 Gene
2024 Parrini E.; Balestrini S.; Rutigliano D.; Ricci M.; Mei D.; Guerrini R.
CDKL-5 encephalopathy in an Indian girl: Partial response to the modified Atkins diet
2017 Sharma, Suvasini*; Goel, Shaiphali; Jain, Puneet; Marini, Carla; Mei, Davide
CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndrome
2023 Nicola Specchio , Marina Trivisano , Matteo Lenge , Alessandro Ferretti , Davide Mei , Elena Parrini , Antonio Napolitano , Camilla Rossi-Espagnet , Giacomo Talenti , Daniela Longo , Jacopo Proietti , Francesca Ragona , Elena Freri , Roberta Solazzi , Tiziana Granata , Francesca Darra , Bernardo Dalla Bernardina , Federico Vigevano , Renzo Guerrini
Clinical and molecular delineation of PUS3-associated neurodevelopmental disorders
2021 Nostvik, Miriam; Kateta, Sarah M.; Schonewolf-Greulich, Bitten; Afenjar, Alexandra; Barth, Magalie; Boschann, Felix; Doummar, Diane; Haack, Tobias B.; Keren, Boris; Livshits, Ludmilla A.; Mei, Davide; Park, Joohyun; Pisano, Tiziana; Prouteau, Clement; Umair, Muhammad; Waqas, Ahmed; Ziegler, Alban; Guerrini, Renzo; Moller, Rikke S.; Tumer, Zeynep
Clinical features and outcome of 6 new patients carrying de novoKCNB1gene mutations
2017 Marini, Carla; Romoli, Michele; Parrini, Elena; Costa, Cinzia; Mei, Davide; Mari, Francesco; Parmeggiani, Lucio; Procopio, Elena; Metitieri, Tiziana; Cellini, Elena; Virdò, Simona; De Vita, Dalila; Gentile, Mattia; Prontera, Paolo; Calabresi, Paolo; Guerrini, Renzo
Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes
2017 Parrini E, Marini C, Mei D, Galuppi A, Cellini E, Pucatti D, Chiti L, Rutigliano D, Bianchini C, Virdò S, De Vita D, Bigoni S, Barba , Mari F, Montomoli M, Pisano T, Rosati A; Clinical Study Group;Guerrini R
Distinct epilepsy phenotypes and response to drugs in KCNA1 gain- and loss-of function variants
2021 Miceli, Francesco; Guerrini, Renzo; Nappi, Mario; Soldovieri, Maria Virginia; Cellini, Elena; Gurnett, Christina A.; Parmeggiani, Lucio; Mei, Davide; Taglialatela, Maurizio
Dravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathies
2019 Mei D, Cetica V, Marini C, Guerrini R,
Early infantile epileptic-dyskinetic encephalopathy due to biallelic PIGP mutations
2020 Vetro A, Pisano T, Chiaro S, Procopio E, Guerra A, Parrini E, Mei D, Virdò S, Mangone G, Azzari C, Guerrini R.
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study
2020 Specchio N.; Pietrafusa N.; Doccini V.; Trivisano M.; Darra F.; Ragona F.; Cossu A.; Spolverato S.; Battaglia D.; Quintiliani M.; Luigia Gambardella M.; Rosati A.; Mei D.; Granata T.; Dalla Bernardina B.; Vigevano F.; Guerrini R.
Endocrinological features and epileptic encephalopathy in COX deficiency due to SCO1 mutations: case series and review of literature
2024 Barbato, Alessandro; Gori, Giulia; Sacchini, Michele; Pochiero, Francesca; Bargiacchi, Sara; Traficante, Giovanna; Palazzo, Viviana; Tiberi, Lucia; Bianchini, Claudia; Mei, Davide; Parrini, Elena; Pisano, Tiziana; Procopio, Elena; Guerrini, Renzo; Peron, Angela; Stagi, Stefano
Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17458 subjects
2020 Niestroj L.-M.; Perez-Palma E.; Howrigan D.P.; Zhou Y.; Cheng F.; Saarentaus E.; Nurnberg P.; Stevelink R.; Daly M.J.; Palotie A.; Lal D.; Feng Y.-C.A.; Abbott L.E.; Tashman K.; Cerrato F.; Churchhouse C.; Gupta N.; Neale B.M.; Berkovic S.F.; Lerche H.; Goldstein D.B.; Lowenstein D.H.; Cavalleri G.L.; Cossette P.; Cotsapas C.; De Jonghe P.; Dixon-Salazar T.; Guerrini R.; Hakonarson H.; Heinzen E.L.; Helbig I.; Kwan P.; Marson A.G.; Petrovski S.; Kamalakaran S.; Sisodiya S.M.; Stewart R.; Weckhuysen S.; Depondt C.; Dlugos D.J.; Scheffer I.E.; Striano P.; Freyer C.; Krause R.; May P.; McKenna K.; Regan B.M.; Leu C.; Bennett C.A.; Bellows S.T.; Johns E.M.C.; MacDonald A.; Shilling H.; Burgess R.; Weckhuysen D.; Bahlo M.; O'Brien T.J.; Todaro M.; Stamberger H.; Andrade D.M.; Sadoway T.R.; Mo K.; Krestel H.; Gallati S.; Papacostas S.S.; Kousiappa I.; Tanteles G.A.; Sterbova K.; Vlckova M.; Sedlackova L.; Lassuthova P.; Martin K.; Rosenow F.; Reif P.S.; Knake S.; Kunz W.S.; Zsurka G.; Elger C.E.; Bauer J.; Rademacher M.; Pendziwiat M.; Muhle H.; Rademacher A.; Van Baalen A.; Von Spiczak S.; Stephani U.; Afawi Z.; Korczyn A.D.; Kanaan M.; Canavati C.; Kurlemann G.; Muller-Schluter K.; Kluger G.; Hausler M.; Blatt I.; Lemke J.R.; Krey I.; Weber Y.G.; Wolking S.; Becker F.; Hengsbach C.; Rau S.; Maisch A.F.; Steinhoff B.J.; Schulze-Bonhage A.; Schubert-Bast S.; Schreiber H.; Borggrafe I.; Schankin C.J.; Mayer T.; Korinthenberg R.; Brockmann K.; Dennig D.; Madeleyn R.; Kalviainen R.; Auvinen P.; Saarela A.; Linnankivi T.; Lehesjoki A.-E.; Rees M.I.; Chung S.-K.; Pickrell W.O.; Powell R.; Schneider N.; Balestrini S.; Zagaglia S.; Braatz V.; Johnson M.R.; Auce P.; Sills G.J.; Baum L.W.; Sham P.C.; Cherny S.S.; Lui C.H.T.; Barisic N.; Delanty N.; Doherty C.P.; Shukralla A.; McCormack M.; El-Naggar H.; Canafoglia L.; Franceschetti S.; Castellotti B.; Granata T.; Zara F.; Iacomino M.; Madia F.; Vari M.S.; Mancardi M.M.; Salpietro V.; Bisulli F.; Tinuper P.; Licchetta L.; Pippucci T.; Stipa C.; Muccioli L.; Minardi R.; Gambardella A.; Labate A.; Annesi G.; Manna L.; Gagliardi M.; Parrini E.; Mei D.; Vetro A.; Bianchini C.; Montomoli M.; Doccini V.; Marini C.; Suzuki T.; Inoue Y.; Yamakawa K.; Tumiene B.; Mameniskiene R.; Utkus A.; Praninskiene R.; Grikiniene J.; Samaitiene R.; Sadleir L.G.; King C.; Mountier E.; Caglayan S.H.; Arslan M.; Yapici Z.; Yis U.; Topaloglu P.; Kara B.; Turkdogan D.; Gundogdu-Eken A.; Bebek N.; Ugur-Iseri S.; Baykan B.; Salman B.; Haryanyan G.; Yucesan E.; Kesim Y.; Ozkara C.; Sheidley B.R.; Shain C.; Poduri A.; Buono R.J.; Ferraro T.N.; Sperling M.R.; Lo W.; Privitera M.; French J.A.; Schachter S.; Kuzniecky R.I.; Devinsky O.; Hegde M.; Khankhanian P.; Helbig K.L.; Ellis C.A.; Spalletta G.; Piras F.; Piras F.; Gili T.; Ciullo V.
Erratum: Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals (The American Journal of Human Genetics (2021) 108(6) (965–982), (S0002929721001403), (10.1016/j.ajhg.2021.04.009))
2021 Motelow J.E.; Povysil G.; Dhindsa R.S.; Stanley K.E.; Allen A.S.; Feng Y.-C.A.; Howrigan D.P.; Abbott L.E.; Tashman K.; Cerrato F.; Cusick C.; Singh T.; Heyne H.; Byrnes A.E.; Churchhouse C.; Watts N.; Solomonson M.; Lal D.; Gupta N.; Neale B.M.; Cavalleri G.L.; Cossette P.; Cotsapas C.; De Jonghe P.; Dixon-Salazar T.; Guerrini R.; Hakonarson H.; Heinzen E.L.; Helbig I.; Kwan P.; Marson A.G.; Petrovski S.; Kamalakaran S.; Sisodiya S.M.; Stewart R.; Weckhuysen S.; Depondt C.; Dlugos D.J.; Scheffer I.E.; Striano P.; Freyer C.; Krause R.; May P.; McKenna K.; Regan B.M.; Bennett C.A.; Leu C.; Leech S.L.; O'Brien T.J.; Todaro M.; Stamberger H.; Andrade D.M.; Ali Q.Z.; Sadoway T.R.; Krestel H.; Schaller A.; Papacostas S.S.; Kousiappa I.; Tanteles G.A.; Christou Y.; Sterbova K.; Vlckova M.; Sedlackova L.; Lassuthova P.; Klein K.M.; Rosenow F.; Reif P.S.; Knake S.; Neubauer B.A.; Zimprich F.; Feucht M.; Reinthaler E.M.; Kunz W.S.; Zsurka G.; Surges R.; Baumgartner T.; von Wrede R.; Pendziwiat M.; Muhle H.; Rademacher A.; van Baalen A.; von Spiczak S.; Stephani U.; Afawi Z.; Korczyn A.D.; Kanaan M.; Canavati C.; Kurlemann G.; Muller-Schluter K.; Kluger G.; Hausler M.; Blatt I.; Lemke J.R.; Krey I.; Weber Y.G.; Wolking S.; Becker F.; Lauxmann S.; Bosselmann C.; Kegele J.; Hengsbach C.; Rau S.; Steinhoff B.J.; Schulze-Bonhage A.; Borggrafe I.; Schankin C.J.; Schubert-Bast S.; Schreiber H.; Mayer T.; Korinthenberg R.; Brockmann K.; Wolff M.; Dennig D.; Madeleyn R.; Kalviainen R.; Saarela A.; Timonen O.; Linnankivi T.; Lehesjoki A.-E.; Rheims S.; Lesca G.; Ryvlin P.; Maillard L.; Valton L.; Derambure P.; Bartolomei F.; Hirsch E.; Michel V.; Chassoux F.; Rees M.I.; Chung S.-K.; Pickrell W.O.; Powell R.; Baker M.D.; Fonferko-Shadrach B.; Lawthom C.; Anderson J.; Schneider N.; Balestrini S.; Zagaglia S.; Braatz V.; Johnson M.R.; Auce P.; Sills G.J.; Baum L.W.; Sham P.C.; Cherny S.S.; Lui C.H.T.; Delanty N.; Doherty C.P.; Shukralla A.; El-Naggar H.; Widdess-Walsh P.; Barisic N.; Canafoglia L.; Franceschetti S.; Castellotti B.; Granata T.; Ragona F.; Zara F.; Iacomino M.; Riva A.; Madia F.; Vari M.S.; Salpietro V.; Scala M.; Mancardi M.M.; Nobili L.; Amadori E.; Giacomini T.; Bisulli F.; Pippucci T.; Licchetta L.; Minardi R.; Tinuper P.; Muccioli L.; Mostacci B.; Gambardella A.; Labate A.; Annesi G.; Manna L.; Gagliardi M.; Parrini E.; Mei D.; Vetro A.; Bianchini C.; Montomoli M.; Doccini V.; Barba C.; Hirose S.; Ishii A.; Suzuki T.; Inoue Y.; Yamakawa K.; Beydoun A.; Nasreddine W.; Khoueiry Zgheib N.; Tumiene B.; Utkus A.; Sadleir L.G.; King C.; Caglayan S.H.; Arslan M.; Yapici Z.; Topaloglu P.; Kara B.; Yis U.; Turkdogan D.; Gundogdu-Eken A.; Bebek N.; Ugur-Iseri S.; Baykan B.; Salman B.; Haryanyan G.; Yucesan E.; Kesim Y.; Ozkara C.; Tsai M.-H.; Ho C.-J.; Lin C.-H.; Lin K.-L.; Chou I.-J.; Poduri A.; Shiedley B.R.; Shain C.; Noebels J.L.; Goldman A.; Busch R.M.; Jehi L.; Najm I.M.; Ferguson L.; Khoury J.; Glauser T.A.; Clark P.O.; Buono R.J.; Ferraro T.N.; Sperling M.R.; Lo W.; Privitera M.; French J.A.; Schachter S.; Kuzniecky R.I.; Devinsky O.; Hegde M.; Greenberg D.A.; Ellis C.A.; Goldberg E.; Helbig K.L.; Cosico M.; Vaidiswaran P.; Fitch E.; Berkovic S.F.; Lerche H.; Lowenstein D.H.; Goldstein D.B.
Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G Mutations
2020 Barresi S, Dentici ML, Manzoni F, Bellacchio E, Agolini E, Pizzi S, Ciolfi A, Tarnopolsky M, Brady L, Garone G, Novelli A, Mei D, Guerrini R,Capuano A, Pantaleoni C, Tartaglia M
Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice
2023 Sarah E Sheppard , Laura Bryant , Rochelle N Wickramasekara , Courtney Vaccaro , Brynn Robertson , Jodi Hallgren , Jason Hulen , Cynthia J Watson , Victor Faundes , Yannis Duffourd , Pearl Lee , M Celeste Simon , Xavier de la Cruz , Natália Padilla , Marco Flores-Mendez , Naiara Akizu , Jacqueline Smiler , Renata Pellegrino Da Silva , Dong Li , Michael March , Abdias Diaz-Rosado , Isabella Peixoto de Barcelos , Zhao Xiang Choa , Chin Yan Lim , Christèle Dubourg , Hubert Journel , Florence Demurger , Maureen Mulhern , Cigdem Akman , Natalie Lippa , Marisa Andrews , Dustin Baldridge , John Constantino , Arie van Haeringen , Irina Snoeck-Streef , Penny Chow , Anne Hing , John M Graham Jr , Margaret Au , Laurence Faivre , Wei Shen , Rong Mao , Janice Palumbos , David Viskochil , William Gahl , Cynthia Tifft , Ellen Macnamara , Natalie Hauser , Rebecca Miller , Jessica Maffeo , Alexandra Afenjar , Diane Doummar , Boris Keren , Pamela Arn Sarah Macklin-Mantia , Ilse Meerschaut , Bert Callewaert , André Reis , Christiane Zweier , Carole Brewer , Anand Saggar , Marie F Smeland , Ajith Kumar , Frances Elmslie , Charu Deshpande , Mathilde Nizon , Benjamin Cogne , Yvette van Ierland , Martina Wilke , Marjon van Slegtenhorst , Suzanne Koudijs , Jin Yun Chen , David Dredge , Danielle Pier , Saskia Wortmann , Erik-Jan Kamsteeg , Johannes Koch , Devon Haynes , Lynda Pollack , Hannah Titheradge , Kara Ranguin , Anne-Sophie Denommé-Pichon , Sacha Weber , Rubén Pérez de la Fuente , Jaime Sánchez Del Pozo , Jose Miguel Lezana Rosales , Pascal Joset , Katharina Steindl , Anita Rauch , Davide Mei ,Francesco Mari , Renzo Guerrini , James Lespinasse , Frédéric Tran Mau-Them , Christophe Philippe , Benjamin Dauriat , Laure Raymond , Sébastien Moutton , Anna M Cueto-González , Tiong Yang Tan , Cyril Mignot, Sarah Grotto , Florence Renaldo , Theodore G Drivas , Laura Hennessy , Anna Raper , Ilaria Parenti, Frank J Kaiser , Alma Kuechler , Øyvind L Busk , Lily Islam , Jacob A Siedlik , Lindsay B Henderson , Jane Juusola , Richard Person , Rhonda E Schnur , Antonio Vitobello , Siddharth Banka , Elizabeth J Bhoj , Holly A F Stessman
Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
2023 Daniel G Calame 1 , Tianyu Guo 2 , Chen Wang 2 , Lillian Garrett 3 , Angad Jolly 4 , Moez Dawood 5 , Alina Kurolap 6 , Noa Zunz Henig 6 , Jawid M Fatih , Isabella Herman , Haowei Du , Tadahiro Mitani , Lore Becker , Birgit Rathkolb , Raffaele Gerlini , Claudia Seisenberger , Susan Marschall , Jill V Hunter , Amanda Gerard , Alexis Heidlebaugh , Thomas Challman , Rebecca C Spillmann , Shalini N Jhangiani , Zeynep Coban-Akdemir , Seema Lalani , Lingxiao Liu , Anya Revah-Politi , Alejandro Iglesias , Edwin Guzman , Evan Baugh , Nathalie Boddaert , Sophie Rondeau , Clothide Ormieres , Giulia Barcia , Queenie K G Tan , Isabelle Thiffault , Tomi Pastinen , Kazim Sheikh , Suur Biliciler , Davide Mei , Federico Melani , Vandana Shashi , Yuval Yaron , Mary Steele , Emma Wakeling , Elsebet Østergaard , Lusine Nazaryan-Petersen ; Undiagnosed Diseases Network; Francisca Millan , Teresa Santiago-Sim , Julien Thevenon , Ange-Line Bruel , Christel Thauvin-Robinet , Denny Popp , Konrad Platzer , Pawel Gawlinski , Wojciech Wiszniewski , Dana Marafi , Davut Pehlivan , Jennifer E Posey , Richard A Gibbs , Valerie Gailus-Durner , Renzo Guerrini , Helmut Fuchs , Martin Hrabě de Angelis , Sabine M Hölter , Hoi-Hung Cheung , Shen Gu , James R Lupski
Morphometry and network-based atrophy patterns in SCN1A-related Dravet syndrome
2023 Matteo Lenge , Simona Balestrini , Davide Mei , Letizia Macconi , Maria Eugenia Caligiuri , Valeria Cuccarini , Domenico Aquino , Federica Mazzi , Ludovico d'Incerti , Francesca Darra , Bernardo Dalla Bernardina , Renzo Guerrini
Morquio B disease: From pathophysiology towards diagnosis
2021 Caciotti, Anna; Cellai, Lucrezia; Tonin, Rodolfo; Mei, Davide; Procopio, Elena; Di Rocco, Maja; Andaloro, Antonio; Antuzzi, Daniela; Rampazzo, Angelica; Rigoldi, Miriam; Forni, Giulia; la Marca, Giancarlo; Guerrini, Renzo; Morrone, Amelia
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations | 2017 | Zhu X, Padmanabhan R, Copeland B, Bridgers J, Ren Z, Kamalakaran S, O'Driscoll-Collins A, Berkovic SF, Scheffer IE, Poduri A, Mei D, Guerrini R, Lowenstein DH, Allen AS, Heinzen EL, Goldstein DB | |
| Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course | 2019 | Alessandro Esposito, Antonio Falace, Matias Wagner, Moran Gal, Davide Mei, Valerio Conti, Tiziana Pisano, Davide Aprile, Maria Sabina Cerullo, Antonio De Fusco, Silvia Giovedì, Annette Seibt, Daniella Magen, Tilman Polster, Ayelet Eran, Sarah L Stenton, Chiara Fiorillo, Sarit Ravid, Ertan Mayatepek, Hava Hafner, Saskia Wortmann, Erez Y Levanon, Carla Marini, Hanna Mandel, Fabio Benfenati, Felix Distelmaier, Anna Fassio, Renzo Guerrini | |
| Bilateral Perisylvian Polymicrogyria, Intellectual Disability and Nephronophthisis Associated With Compound Heterozygous Pathogenic Variants in the CEP83 Gene | 2024 | Parrini E.; Balestrini S.; Rutigliano D.; Ricci M.; Mei D.; Guerrini R. | |
| CDKL-5 encephalopathy in an Indian girl: Partial response to the modified Atkins diet | 2017 | Sharma, Suvasini*; Goel, Shaiphali; Jain, Puneet; Marini, Carla; Mei, Davide | |
| CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndrome | 2023 | Nicola Specchio , Marina Trivisano , Matteo Lenge , Alessandro Ferretti , Davide Mei , Elena Parrini , Antonio Napolitano , Camilla Rossi-Espagnet , Giacomo Talenti , Daniela Longo , Jacopo Proietti , Francesca Ragona , Elena Freri , Roberta Solazzi , Tiziana Granata , Francesca Darra , Bernardo Dalla Bernardina , Federico Vigevano , Renzo Guerrini | |
| Clinical and molecular delineation of PUS3-associated neurodevelopmental disorders | 2021 | Nostvik, Miriam; Kateta, Sarah M.; Schonewolf-Greulich, Bitten; Afenjar, Alexandra; Barth, Magalie; Boschann, Felix; Doummar, Diane; Haack, Tobias B.; Keren, Boris; Livshits, Ludmilla A.; Mei, Davide; Park, Joohyun; Pisano, Tiziana; Prouteau, Clement; Umair, Muhammad; Waqas, Ahmed; Ziegler, Alban; Guerrini, Renzo; Moller, Rikke S.; Tumer, Zeynep | |
| Clinical features and outcome of 6 new patients carrying de novoKCNB1gene mutations | 2017 | Marini, Carla; Romoli, Michele; Parrini, Elena; Costa, Cinzia; Mei, Davide; Mari, Francesco; Parmeggiani, Lucio; Procopio, Elena; Metitieri, Tiziana; Cellini, Elena; Virdò, Simona; De Vita, Dalila; Gentile, Mattia; Prontera, Paolo; Calabresi, Paolo; Guerrini, Renzo | |
| Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes | 2017 | Parrini E, Marini C, Mei D, Galuppi A, Cellini E, Pucatti D, Chiti L, Rutigliano D, Bianchini C, Virdò S, De Vita D, Bigoni S, Barba , Mari F, Montomoli M, Pisano T, Rosati A; Clinical Study Group;Guerrini R | |
| Distinct epilepsy phenotypes and response to drugs in KCNA1 gain- and loss-of function variants | 2021 | Miceli, Francesco; Guerrini, Renzo; Nappi, Mario; Soldovieri, Maria Virginia; Cellini, Elena; Gurnett, Christina A.; Parmeggiani, Lucio; Mei, Davide; Taglialatela, Maurizio | |
| Dravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathies | 2019 | Mei D, Cetica V, Marini C, Guerrini R, | |
| Early infantile epileptic-dyskinetic encephalopathy due to biallelic PIGP mutations | 2020 | Vetro A, Pisano T, Chiaro S, Procopio E, Guerra A, Parrini E, Mei D, Virdò S, Mangone G, Azzari C, Guerrini R. | |
| Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study | 2020 | Specchio N.; Pietrafusa N.; Doccini V.; Trivisano M.; Darra F.; Ragona F.; Cossu A.; Spolverato S.; Battaglia D.; Quintiliani M.; Luigia Gambardella M.; Rosati A.; Mei D.; Granata T.; Dalla Bernardina B.; Vigevano F.; Guerrini R. | |
| Endocrinological features and epileptic encephalopathy in COX deficiency due to SCO1 mutations: case series and review of literature | 2024 | Barbato, Alessandro; Gori, Giulia; Sacchini, Michele; Pochiero, Francesca; Bargiacchi, Sara; Traficante, Giovanna; Palazzo, Viviana; Tiberi, Lucia; Bianchini, Claudia; Mei, Davide; Parrini, Elena; Pisano, Tiziana; Procopio, Elena; Guerrini, Renzo; Peron, Angela; Stagi, Stefano | |
| Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17458 subjects | 2020 | Niestroj L.-M.; Perez-Palma E.; Howrigan D.P.; Zhou Y.; Cheng F.; Saarentaus E.; Nurnberg P.; Stevelink R.; Daly M.J.; Palotie A.; Lal D.; Feng Y.-C.A.; Abbott L.E.; Tashman K.; Cerrato F.; Churchhouse C.; Gupta N.; Neale B.M.; Berkovic S.F.; Lerche H.; Goldstein D.B.; Lowenstein D.H.; Cavalleri G.L.; Cossette P.; Cotsapas C.; De Jonghe P.; Dixon-Salazar T.; Guerrini R.; Hakonarson H.; Heinzen E.L.; Helbig I.; Kwan P.; Marson A.G.; Petrovski S.; Kamalakaran S.; Sisodiya S.M.; Stewart R.; Weckhuysen S.; Depondt C.; Dlugos D.J.; Scheffer I.E.; Striano P.; Freyer C.; Krause R.; May P.; McKenna K.; Regan B.M.; Leu C.; Bennett C.A.; Bellows S.T.; Johns E.M.C.; MacDonald A.; Shilling H.; Burgess R.; Weckhuysen D.; Bahlo M.; O'Brien T.J.; Todaro M.; Stamberger H.; Andrade D.M.; Sadoway T.R.; Mo K.; Krestel H.; Gallati S.; Papacostas S.S.; Kousiappa I.; Tanteles G.A.; Sterbova K.; Vlckova M.; Sedlackova L.; Lassuthova P.; Martin K.; Rosenow F.; Reif P.S.; Knake S.; Kunz W.S.; Zsurka G.; Elger C.E.; Bauer J.; Rademacher M.; Pendziwiat M.; Muhle H.; Rademacher A.; Van Baalen A.; Von Spiczak S.; Stephani U.; Afawi Z.; Korczyn A.D.; Kanaan M.; Canavati C.; Kurlemann G.; Muller-Schluter K.; Kluger G.; Hausler M.; Blatt I.; Lemke J.R.; Krey I.; Weber Y.G.; Wolking S.; Becker F.; Hengsbach C.; Rau S.; Maisch A.F.; Steinhoff B.J.; Schulze-Bonhage A.; Schubert-Bast S.; Schreiber H.; Borggrafe I.; Schankin C.J.; Mayer T.; Korinthenberg R.; Brockmann K.; Dennig D.; Madeleyn R.; Kalviainen R.; Auvinen P.; Saarela A.; Linnankivi T.; Lehesjoki A.-E.; Rees M.I.; Chung S.-K.; Pickrell W.O.; Powell R.; Schneider N.; Balestrini S.; Zagaglia S.; Braatz V.; Johnson M.R.; Auce P.; Sills G.J.; Baum L.W.; Sham P.C.; Cherny S.S.; Lui C.H.T.; Barisic N.; Delanty N.; Doherty C.P.; Shukralla A.; McCormack M.; El-Naggar H.; Canafoglia L.; Franceschetti S.; Castellotti B.; Granata T.; Zara F.; Iacomino M.; Madia F.; Vari M.S.; Mancardi M.M.; Salpietro V.; Bisulli F.; Tinuper P.; Licchetta L.; Pippucci T.; Stipa C.; Muccioli L.; Minardi R.; Gambardella A.; Labate A.; Annesi G.; Manna L.; Gagliardi M.; Parrini E.; Mei D.; Vetro A.; Bianchini C.; Montomoli M.; Doccini V.; Marini C.; Suzuki T.; Inoue Y.; Yamakawa K.; Tumiene B.; Mameniskiene R.; Utkus A.; Praninskiene R.; Grikiniene J.; Samaitiene R.; Sadleir L.G.; King C.; Mountier E.; Caglayan S.H.; Arslan M.; Yapici Z.; Yis U.; Topaloglu P.; Kara B.; Turkdogan D.; Gundogdu-Eken A.; Bebek N.; Ugur-Iseri S.; Baykan B.; Salman B.; Haryanyan G.; Yucesan E.; Kesim Y.; Ozkara C.; Sheidley B.R.; Shain C.; Poduri A.; Buono R.J.; Ferraro T.N.; Sperling M.R.; Lo W.; Privitera M.; French J.A.; Schachter S.; Kuzniecky R.I.; Devinsky O.; Hegde M.; Khankhanian P.; Helbig K.L.; Ellis C.A.; Spalletta G.; Piras F.; Piras F.; Gili T.; Ciullo V. | |
| Erratum: Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals (The American Journal of Human Genetics (2021) 108(6) (965–982), (S0002929721001403), (10.1016/j.ajhg.2021.04.009)) | 2021 | Motelow J.E.; Povysil G.; Dhindsa R.S.; Stanley K.E.; Allen A.S.; Feng Y.-C.A.; Howrigan D.P.; Abbott L.E.; Tashman K.; Cerrato F.; Cusick C.; Singh T.; Heyne H.; Byrnes A.E.; Churchhouse C.; Watts N.; Solomonson M.; Lal D.; Gupta N.; Neale B.M.; Cavalleri G.L.; Cossette P.; Cotsapas C.; De Jonghe P.; Dixon-Salazar T.; Guerrini R.; Hakonarson H.; Heinzen E.L.; Helbig I.; Kwan P.; Marson A.G.; Petrovski S.; Kamalakaran S.; Sisodiya S.M.; Stewart R.; Weckhuysen S.; Depondt C.; Dlugos D.J.; Scheffer I.E.; Striano P.; Freyer C.; Krause R.; May P.; McKenna K.; Regan B.M.; Bennett C.A.; Leu C.; Leech S.L.; O'Brien T.J.; Todaro M.; Stamberger H.; Andrade D.M.; Ali Q.Z.; Sadoway T.R.; Krestel H.; Schaller A.; Papacostas S.S.; Kousiappa I.; Tanteles G.A.; Christou Y.; Sterbova K.; Vlckova M.; Sedlackova L.; Lassuthova P.; Klein K.M.; Rosenow F.; Reif P.S.; Knake S.; Neubauer B.A.; Zimprich F.; Feucht M.; Reinthaler E.M.; Kunz W.S.; Zsurka G.; Surges R.; Baumgartner T.; von Wrede R.; Pendziwiat M.; Muhle H.; Rademacher A.; van Baalen A.; von Spiczak S.; Stephani U.; Afawi Z.; Korczyn A.D.; Kanaan M.; Canavati C.; Kurlemann G.; Muller-Schluter K.; Kluger G.; Hausler M.; Blatt I.; Lemke J.R.; Krey I.; Weber Y.G.; Wolking S.; Becker F.; Lauxmann S.; Bosselmann C.; Kegele J.; Hengsbach C.; Rau S.; Steinhoff B.J.; Schulze-Bonhage A.; Borggrafe I.; Schankin C.J.; Schubert-Bast S.; Schreiber H.; Mayer T.; Korinthenberg R.; Brockmann K.; Wolff M.; Dennig D.; Madeleyn R.; Kalviainen R.; Saarela A.; Timonen O.; Linnankivi T.; Lehesjoki A.-E.; Rheims S.; Lesca G.; Ryvlin P.; Maillard L.; Valton L.; Derambure P.; Bartolomei F.; Hirsch E.; Michel V.; Chassoux F.; Rees M.I.; Chung S.-K.; Pickrell W.O.; Powell R.; Baker M.D.; Fonferko-Shadrach B.; Lawthom C.; Anderson J.; Schneider N.; Balestrini S.; Zagaglia S.; Braatz V.; Johnson M.R.; Auce P.; Sills G.J.; Baum L.W.; Sham P.C.; Cherny S.S.; Lui C.H.T.; Delanty N.; Doherty C.P.; Shukralla A.; El-Naggar H.; Widdess-Walsh P.; Barisic N.; Canafoglia L.; Franceschetti S.; Castellotti B.; Granata T.; Ragona F.; Zara F.; Iacomino M.; Riva A.; Madia F.; Vari M.S.; Salpietro V.; Scala M.; Mancardi M.M.; Nobili L.; Amadori E.; Giacomini T.; Bisulli F.; Pippucci T.; Licchetta L.; Minardi R.; Tinuper P.; Muccioli L.; Mostacci B.; Gambardella A.; Labate A.; Annesi G.; Manna L.; Gagliardi M.; Parrini E.; Mei D.; Vetro A.; Bianchini C.; Montomoli M.; Doccini V.; Barba C.; Hirose S.; Ishii A.; Suzuki T.; Inoue Y.; Yamakawa K.; Beydoun A.; Nasreddine W.; Khoueiry Zgheib N.; Tumiene B.; Utkus A.; Sadleir L.G.; King C.; Caglayan S.H.; Arslan M.; Yapici Z.; Topaloglu P.; Kara B.; Yis U.; Turkdogan D.; Gundogdu-Eken A.; Bebek N.; Ugur-Iseri S.; Baykan B.; Salman B.; Haryanyan G.; Yucesan E.; Kesim Y.; Ozkara C.; Tsai M.-H.; Ho C.-J.; Lin C.-H.; Lin K.-L.; Chou I.-J.; Poduri A.; Shiedley B.R.; Shain C.; Noebels J.L.; Goldman A.; Busch R.M.; Jehi L.; Najm I.M.; Ferguson L.; Khoury J.; Glauser T.A.; Clark P.O.; Buono R.J.; Ferraro T.N.; Sperling M.R.; Lo W.; Privitera M.; French J.A.; Schachter S.; Kuzniecky R.I.; Devinsky O.; Hegde M.; Greenberg D.A.; Ellis C.A.; Goldberg E.; Helbig K.L.; Cosico M.; Vaidiswaran P.; Fitch E.; Berkovic S.F.; Lerche H.; Lowenstein D.H.; Goldstein D.B. | |
| Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G Mutations | 2020 | Barresi S, Dentici ML, Manzoni F, Bellacchio E, Agolini E, Pizzi S, Ciolfi A, Tarnopolsky M, Brady L, Garone G, Novelli A, Mei D, Guerrini R,Capuano A, Pantaleoni C, Tartaglia M | |
| Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice | 2023 | Sarah E Sheppard , Laura Bryant , Rochelle N Wickramasekara , Courtney Vaccaro , Brynn Robertson , Jodi Hallgren , Jason Hulen , Cynthia J Watson , Victor Faundes , Yannis Duffourd , Pearl Lee , M Celeste Simon , Xavier de la Cruz , Natália Padilla , Marco Flores-Mendez , Naiara Akizu , Jacqueline Smiler , Renata Pellegrino Da Silva , Dong Li , Michael March , Abdias Diaz-Rosado , Isabella Peixoto de Barcelos , Zhao Xiang Choa , Chin Yan Lim , Christèle Dubourg , Hubert Journel , Florence Demurger , Maureen Mulhern , Cigdem Akman , Natalie Lippa , Marisa Andrews , Dustin Baldridge , John Constantino , Arie van Haeringen , Irina Snoeck-Streef , Penny Chow , Anne Hing , John M Graham Jr , Margaret Au , Laurence Faivre , Wei Shen , Rong Mao , Janice Palumbos , David Viskochil , William Gahl , Cynthia Tifft , Ellen Macnamara , Natalie Hauser , Rebecca Miller , Jessica Maffeo , Alexandra Afenjar , Diane Doummar , Boris Keren , Pamela Arn Sarah Macklin-Mantia , Ilse Meerschaut , Bert Callewaert , André Reis , Christiane Zweier , Carole Brewer , Anand Saggar , Marie F Smeland , Ajith Kumar , Frances Elmslie , Charu Deshpande , Mathilde Nizon , Benjamin Cogne , Yvette van Ierland , Martina Wilke , Marjon van Slegtenhorst , Suzanne Koudijs , Jin Yun Chen , David Dredge , Danielle Pier , Saskia Wortmann , Erik-Jan Kamsteeg , Johannes Koch , Devon Haynes , Lynda Pollack , Hannah Titheradge , Kara Ranguin , Anne-Sophie Denommé-Pichon , Sacha Weber , Rubén Pérez de la Fuente , Jaime Sánchez Del Pozo , Jose Miguel Lezana Rosales , Pascal Joset , Katharina Steindl , Anita Rauch , Davide Mei ,Francesco Mari , Renzo Guerrini , James Lespinasse , Frédéric Tran Mau-Them , Christophe Philippe , Benjamin Dauriat , Laure Raymond , Sébastien Moutton , Anna M Cueto-González , Tiong Yang Tan , Cyril Mignot, Sarah Grotto , Florence Renaldo , Theodore G Drivas , Laura Hennessy , Anna Raper , Ilaria Parenti, Frank J Kaiser , Alma Kuechler , Øyvind L Busk , Lily Islam , Jacob A Siedlik , Lindsay B Henderson , Jane Juusola , Richard Person , Rhonda E Schnur , Antonio Vitobello , Siddharth Banka , Elizabeth J Bhoj , Holly A F Stessman | |
| Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease | 2023 | Daniel G Calame 1 , Tianyu Guo 2 , Chen Wang 2 , Lillian Garrett 3 , Angad Jolly 4 , Moez Dawood 5 , Alina Kurolap 6 , Noa Zunz Henig 6 , Jawid M Fatih , Isabella Herman , Haowei Du , Tadahiro Mitani , Lore Becker , Birgit Rathkolb , Raffaele Gerlini , Claudia Seisenberger , Susan Marschall , Jill V Hunter , Amanda Gerard , Alexis Heidlebaugh , Thomas Challman , Rebecca C Spillmann , Shalini N Jhangiani , Zeynep Coban-Akdemir , Seema Lalani , Lingxiao Liu , Anya Revah-Politi , Alejandro Iglesias , Edwin Guzman , Evan Baugh , Nathalie Boddaert , Sophie Rondeau , Clothide Ormieres , Giulia Barcia , Queenie K G Tan , Isabelle Thiffault , Tomi Pastinen , Kazim Sheikh , Suur Biliciler , Davide Mei , Federico Melani , Vandana Shashi , Yuval Yaron , Mary Steele , Emma Wakeling , Elsebet Østergaard , Lusine Nazaryan-Petersen ; Undiagnosed Diseases Network; Francisca Millan , Teresa Santiago-Sim , Julien Thevenon , Ange-Line Bruel , Christel Thauvin-Robinet , Denny Popp , Konrad Platzer , Pawel Gawlinski , Wojciech Wiszniewski , Dana Marafi , Davut Pehlivan , Jennifer E Posey , Richard A Gibbs , Valerie Gailus-Durner , Renzo Guerrini , Helmut Fuchs , Martin Hrabě de Angelis , Sabine M Hölter , Hoi-Hung Cheung , Shen Gu , James R Lupski | |
| Morphometry and network-based atrophy patterns in SCN1A-related Dravet syndrome | 2023 | Matteo Lenge , Simona Balestrini , Davide Mei , Letizia Macconi , Maria Eugenia Caligiuri , Valeria Cuccarini , Domenico Aquino , Federica Mazzi , Ludovico d'Incerti , Francesca Darra , Bernardo Dalla Bernardina , Renzo Guerrini | |
| Morquio B disease: From pathophysiology towards diagnosis | 2021 | Caciotti, Anna; Cellai, Lucrezia; Tonin, Rodolfo; Mei, Davide; Procopio, Elena; Di Rocco, Maja; Andaloro, Antonio; Antuzzi, Daniela; Rampazzo, Angelica; Rigoldi, Miriam; Forni, Giulia; la Marca, Giancarlo; Guerrini, Renzo; Morrone, Amelia |